Quality-of-life results for accelerated partial breast irradiation with interstitial brachytherapy versus whole-breast irradiation in early breast cancer after breast-conserving surgery (GEC-ESTRO): 5-year results of a randomised, phase 3 trial

Groupe Européen de Curiethérapie of European Society for Radiotherapy and Oncology (GEC-ESTRO)

114 Citations (Scopus)

Abstract

Background: Previous results from the GEC-ESTRO trial showed that accelerated partial breast irradiation (APBI) using multicatheter brachytherapy in the treatment of early breast cancer after breast-conserving surgery was non-inferior to whole-breast irradiation in terms of local control and overall survival. Here, we present 5-year results of patient-reported quality of life. Methods: We did this randomised controlled phase 3 trial at 16 hospitals and medical centres in seven European countries. Patients aged 40 years or older with 0–IIA breast cancer were randomly assigned (1:1) after breast-conserving surgery (resection margins ≥2 mm) to receive either whole-breast irradiation of 50 Gy with a boost of 10 Gy or APBI using multicatheter brachytherapy. Randomisation was stratified by study centre, tumour type, and menopausal status, with a block size of ten and an automated dynamic algorithm. There was no masking of patients or investigators. The primary endpoint of the trial was ipsilateral local recurrence. Here, we present 5-year results of quality of life (a prespecified secondary endpoint). Quality-of-life questionnaires (European Organisation for Research and Treatment of Cancer QLQ-C30, breast cancer module QLQ-BR23) were completed before radiotherapy (baseline 1), immediately after radiotherapy (baseline 2), and during follow-up. We analysed the data according to treatment received (as-treated population). Recruitment was completed in 2009, and long-term follow-up is continuing. The trial is registered at ClinicalTrials.gov, number NCT00402519. Findings: Between April 20, 2004, and July 30, 2009, 633 patients had accelerated partial breast irradiation and 551 patients had whole-breast irradiation. Quality-of-life questionnaires at baseline 1 were available for 334 (53%) of 663 patients in the APBI group and 314 (57%) of 551 patients in the whole-breast irradiation group; the response rate was similar during follow-up. Global health status (range 0–100) was stable in both groups: at baseline 1, APBI group mean score 65·5 (SD 20·6) versus whole-breast irradiation group 64·6 (19·6), p=0·37; at 5 years, APBI group 66·2 (22·2) versus whole-breast irradiation group 66·0 (21·8), p=0·94. The only moderate, significant difference (difference of 10–20 points) between the groups was found in the breast symptoms scale. Breast symptom scores were significantly higher (ie, worse) after whole-breast irradiation than after APBI at baseline 2 (difference of means 13·6, 95% CI 9·7–17·5; p<0·0001) and at 3-month follow-up (difference of means 12·7, 95% CI 9·8–15·6; p<0·0001). Interpretation: APBI with multicatheter brachytherapy was not associated with worse quality of life compared with whole-breast irradiation. This finding supports APBI as an alternative treatment option after breast-conserving surgery for patients with early breast cancer. Funding: German Cancer Aid.

Original languageEnglish
JournalThe Lancet Oncology
Volume19
Issue number6
Pages (from-to)834-844
Number of pages11
ISSN1470-2045
DOIs
Publication statusPublished - 06.2018

Funding

VS received a research grant from German Cancer Aid during the conduct of the trial and consultation fees, grants, and honoraria from Nucletron Operations BV, and Elekta Company, outside the submitted work. OJO reports a grant from German Cancer Aid, and personal fees from Elekta during the conduct of the study. RF received grants, personal fees, and non-financial support from Merck Serono, Fresenius Kabi, Novocure, MSD, and AstraZeneca, outside the submitted work; and personal fees and non-financial support from Brainlab, Sennewald GmbH, and Bristol-Myers Squibb, outside the submitted work. All other authors declare no competing interests. The study was funded by German Cancer Aid. We thank the patients who participated in this trial and all the physicians, nurses, and data managers involved in the study.

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